Clinical Trial Translation Services

Whether or not you need to have your translated clinical trial certified depends on the regulations of the country in which you are conducting the trial. In some countries, it is required that all clinical trial documents be translated and certified by a qualified translator. In other countries, it is only required that certain documents, such as the informed consent form, be translated and certified.

Yes, Tomedes is well-equipped to handle translations for different phases of clinical trials. Our team of expert linguists possesses in-depth knowledge of the medical field and extensive experience in translating clinical trial documents for all phases, from pre-clinical research to post-marketing studies. Whether it's translating protocols, informed consent forms, case report forms, or any other essential documents, we ensure accurate and precise translations to support your clinical research at every stage.

Absolutely! At Tomedes, we understand the importance of maintaining the necessary formatting for clinical trial documents. Our expert translators not only ensure accurate and precise translations but also pay close attention to preserving the original document's layout, formatting, and structure. Whether it's tables, graphs, headers, footers, or any other formatting elements, you can trust us to deliver translated clinical trial documents with the required formatting intact, ready for submission and regulatory compliance.